Reaktion #733411

ord-9e4b7bb9d7a74299aaf5be5f37acc503

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenconcentrated in vacuo
  2. 2
    workup.DISSOLUTIONThe resultant residue was dissolved in Et2O
  3. 3
    Filtrationfiltered
  4. 4
    Einengenthe filtrated was concentrated in vacuo
  5. 5
    SonstigeThis residue was purified by chromatography (silica gel, EtOAc/hexane:5/95)

Vorschrift

A solution of 1-(difluoromethoxy)-4-iodobenzene (12.7 g, 50 mmol) in triethylamine (175 mL) was treated with tetrakis(triphenylphosphine)palladium (4.0 g, 3.5 mmol), copper iodide (925 mg, 4.85 mmol), and a solution of ethynyl(trimethyl)silane (6.9 mL, 50 mmol) in acetonitrile at room temperature, stirred for 1 h at 60° C. and concentrated in vacuo. The resultant residue was dissolved in Et2O, filtered and the filtrated was concentrated in vacuo. This residue was purified by chromatography (silica gel, EtOAc/hexane:5/95) to give {[4-(difluoromethoxy)-phenyl]ethynyl}(trimethyl)silane (11.5 g, 96%) as an oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07705030B2uspto-grants-2010_04